ADHD Medication Dosing in Pediatric Patients
Age-Specific Treatment Approach
For preschool children (ages 4-5 years), behavior therapy should be the first-line treatment, with medication reserved only for those with moderate-to-severe dysfunction who have not responded adequately to behavioral interventions after at least 9 months of persistent symptoms. 1, 2
Preschool-Aged Children (4-5 years)
- When medication is necessary, methylphenidate should be initiated at lower starting doses with smaller incremental increases due to slower metabolism in this age group 1, 2
- Maximum doses have not been adequately studied in preschool-aged children, so caution is warranted 1
- Only children with dysfunction manifested in both home and other settings (preschool/child care) should be considered for medication 1
School-Aged Children (6 years and older)
Stimulant Medications (First-Line Treatment)
Methylphenidate:
- Starting dose: 5 mg twice daily (before breakfast and lunch) 3
- Titration: Increase by 5-10 mg weekly based on clinical response 3
- Maximum daily dose: 60 mg 3
- Dosing should not exceed 2 mg/kg/day 4
Amphetamine/Dextroamphetamine:
- Ages 3-5 years: Start with 2.5 mg daily; increase by 2.5 mg weekly 5
- Ages 6 years and older: Start with 5 mg once or twice daily; increase by 5 mg weekly 5
- Maximum daily dose: 40 mg 5, 2
- Rarely necessary to exceed 40 mg/day 5
- For children weighing less than 20 kg, use caution during titration 2
Lisdexamfetamine (Vyvanse):
- Titration requires 2-4 weeks to reach optimal dosing 6
- Weekly contact should be maintained during initial titration 6
- Maximum dose: 70 mg/day 2
Non-Stimulant Medications (Second-Line or When Stimulants Contraindicated)
Atomoxetine:
- Children/adolescents up to 70 kg: Start at 0.5 mg/kg/day; increase after minimum 3 days to target of 1.2 mg/kg/day 7
- Maximum: 1.4 mg/kg/day or 100 mg, whichever is less 7
- Children/adolescents over 70 kg: Start at 40 mg/day; increase after minimum 3 days to target of 80 mg 7
- May increase to maximum 100 mg after 2-4 additional weeks if optimal response not achieved 7
- Can be given as single morning dose or divided (morning and late afternoon/early evening) 7
Guanfacine Extended-Release:
- Target dose range: 0.05-0.12 mg/kg/day or 1-4 mg/day 2
- Maximum dose: 4 mg daily 2
- Titration: Increase by 1 mg increments weekly based on clinical response 2
Clonidine Extended-Release:
- Alternative non-stimulant option, particularly useful in adolescents with substance abuse concerns or medication diversion risk 1, 2
Adolescents (12-18 years)
Special Considerations
- Screen for substance use symptoms before initiating medication 1
- Monitor for medication diversion (use by parents, classmates, or acquaintances) 1
- Consider non-stimulant medications (atomoxetine, extended-release guanfacine, extended-release clonidine) to minimize abuse potential 1
- Provide medication coverage for driving hours using longer-acting or late-afternoon short-acting medications 1
Titration Protocol
Weekly dose adjustments are standard practice:
- Maintain weekly contact (telephone acceptable) during initial titration 6
- Assess clinical response and tolerability before each dose increase 6
- Use rating scales with age- and gender-specific norms to assess symptoms before treatment and after each major dose adjustment 1
- Systematically assess for side effects including insomnia, anorexia, headaches, weight loss, and mood changes 6
Monitoring Requirements
Growth Parameters
- Monitor weight at each visit to assess for appetite suppression 2, 6
- Closely monitor height and weight in pediatric patients, as long-term growth suppression can occur 3
- Growth attenuation is more pronounced in children requiring higher doses and those starting treatment at younger ages 4
Cardiovascular Monitoring
- Regularly assess blood pressure and pulse, especially at higher doses 2
- Avoid use in patients with known structural cardiac abnormalities, cardiomyopathy, serious cardiac arrhythmias, coronary artery disease, or other serious cardiac disease 3
Psychiatric Monitoring
- Screen for personal or family history of bipolar disorder, mania, or hypomania before initiating treatment 7
- Monitor for emergence of psychotic or manic symptoms 3
- For atomoxetine specifically, monitor closely for suicidality, clinical worsening, and unusual behavioral changes 2
Special Dosing Adjustments
Hepatic Impairment (Atomoxetine)
- Moderate hepatic insufficiency (Child-Pugh Class B): Reduce initial and target doses to 50% of normal 7
- Severe hepatic insufficiency (Child-Pugh Class C): Reduce initial and target doses to 25% of normal 7
CYP2D6 Poor Metabolizers or Strong Inhibitor Use (Atomoxetine)
- Children/adolescents up to 70 kg: Start at 0.5 mg/kg/day; increase to 1.2 mg/kg/day only if symptoms fail to improve after 4 weeks and initial dose is well tolerated 7
- Children/adolescents over 70 kg and adults: Start at 40 mg/day; increase to 80 mg/day only if symptoms fail to improve after 4 weeks and initial dose is well tolerated 7
Common Pitfalls to Avoid
- Starting at too high a dose leads to unnecessary side effects and decreased medication adherence 6
- Failure to systematically assess both benefits and side effects during titration 6
- Not using standardized rating scales to objectively measure treatment response 1
- Administering late evening doses of stimulants, which causes insomnia 5
- Failing to screen for cardiac disease, bipolar disorder, or substance use before initiating treatment 1, 3, 7
Extended-Release Formulations
- Extended-release preparations provide 8-12 hours of symptom control with once-daily dosing 8, 9
- 8-hour preparations (Metadate CD, Ritalin LA) utilize microbead technology 8
- 12-hour preparation (Concerta) utilizes osmotic pump system 8
- All extended-release formulations are equally efficacious in controlling ADHD symptoms 9
- Capsule formulations can be opened and sprinkled on applesauce for patients with difficulty swallowing 9